MODULAR CENTER PEGGED GLENOID

Abstract

A glenoid component used for shoulder arthroplasty is adapted to be implanted into a scapula and engaged by a head of a humeral component. The glenoid component includes a body having a first articulating surface and a second medial surface opposite to the first articulating surface. The first articulating surface is adapted to engage with a humeral head. A plurality of removable fixed pegs each have a first end adapted to engage a cavity formed in the scapula and a second end extending from the medial surface. A central peg fixation mechanism is provided that is configured to couple an optional central fixation peg to the medial surface.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part application of U.S. patent application Ser. No. 11/385,035, filed on Mar. 20, 2006, now U.S. Pat. No. ______, issued on ______. The entire disclosure of the above application is incorporated herein by reference.

FIELD

The present disclosure relates to a prosthetic device and, more particularly, to a modular glenoid prosthetic.

BACKGROUND

The statements in this section merely provide background information related to the present disclosure and may not constitute prior art. A natural shoulder joint may undergo degenerative changes due to a variety of etiologies. When these degenerative changes become so far advanced and irreversible, it may ultimately become necessary to replace a natural shoulder joint with a prosthetic shoulder joint. When implantation of such a shoulder joint prosthesis becomes necessary, the natural head portion of the humerus can be resected and a cavity is created in the intramedullary canal of the host humerus for accepting a humeral component. The humeral component includes a head portion used to replace the natural head of the humerus. Once the humeral component has been implanted, the glenoid cavity positioned at the lateral edge of the scapula may also be resurfaced and shaped to accept a glenoid component. The glenoid component generally includes an articulating surface which is engaged by the head portion of the humeral component.

It is generally known in the art to provide a shoulder joint prosthesis having a glenoid component, as discussed above. However, the current prior art glenoid components along with the associated surgical components and instruments utilized during shoulder arthroplasty suffer from many disadvantages.

For example, since the glenoid component is subject to various types of loading by the head portion of the humeral component, the glenoid component must offer a stable and secure articulating surface. To achieve this, some glenoid components provide pegs that are inserted and cemented into holes bored into the glenoid cavity. However, such existing pegged glenoid components also exhibit several disadvantages. For example, some of the pegged glenoid components utilize up to five pegs to stabilize and secure the glenoid component to the scapula. Such glenoid components increase the amount of bone tissue removed, while also increasing the labor and complexity of the shoulder arthroplasty. Other pegged glenoid components may offer one or two larger diameter pegs that reduce the complexity of the shoulder arthroplasty. However, the larger diameter pegs also requires excess bone tissue to be removed that may not be practical in some patients. Furthermore, the use of one or two pegs may potentially reduce overall stability of the glenoid component, similar to a keeled glenoid.

Additionally, most prior art glenoid components only rely on the keel or pegs to secure the glenoid component to the scapula, via a cement mantle. These systems are typically rigid in fixation methods. In this regard, the prior art systems fail to provide a selection of coupling mechanisms which may best be used to address varying degenerative changes or specific muscular needs of a patient.

What is needed then is a glenoid component and associated surgical components for use in shoulder arthroplasty that does not suffer from the above-mentioned disadvantages. This in turn, will provide a glenoid component which is stable and secure, reduces the overall amount of bone tissue required to be removed, reduces inventory, reduces the overall surgical time and complexity, increases overall medial surface area, enhances and increases attachment strength and adaptivity without increasing overall peg diameter, provides a fully enhanced coupling mechanism and increased overall stability, and provides increased tensile and shear strength. It is, therefore, an object of the present invention to provide such a glenoid component and associated surgical components for use in shoulder arthroplasty.

SUMMARY

In accordance with the teachings of the present invention, an apparatus and method for shoulder arthroplasty is disclosed. The apparatus and method employs a glenoid component and other associated surgical components for use in the shoulder arthroplasty. In this regard, the glenoid component is adapted to be implanted into a scapula at the glenoid fossa or cavity and engaged by a head portion of a humeral component.

In one embodiment, a glenoid component is used for shoulder arthroplasty such that the glenoid component is adapted to be implanted into a scapula and engaged by a head of a humeral component. The glenoid component includes a body having a first articulating surface and a second medial surface opposite to the first articulating surface. The first articulating surface is adapted to be engaged by the head of the humeral component and the second medial surface is adapted to be secured to the scapula. A plurality of fixed pegs are provided, each having a first end adapted to engage a cavity formed in the scapula and a second end extending from the medial surface. A central peg fixation mechanism is provided that is configured to couple a central fixation peg to the medial surface.

In another embodiment, a system for use during shoulder arthroplasty is provided. The system has a glenoid component adapted to be implanted into a scapula and engaged by a head of a humeral component. The glenoid component includes, a body having a first spherical articulating surface and a second medial surface. The first spherical articulating surface is adapted to permit rotational movement of the head of the humeral component. A plurality of fixed coupling pegs are provided having a first end adapted to engage a cavity formed in the scapula. The medial portion has a central stem fixation mechanism, and a depending central stem.

In another embodiment, a method for implanting a medical device is disclosed. A glenoid prosthetic having a plurality of fixed pegs and a center fixation peg coupling mechanism is provided. The method includes machining a scapula to form a resected glenoid. A plurality of fixed peg accepting holes are machined in the resected glenoid. Further, the scapula is machined to form a center fixation peg coupling member accepting aperture. The physician will then determine if a center fixation peg is needed. If a center peg is required, a center peg is coupled to a glenoid prosthetic. A central peg accepting aperture is optionally machined into the resected glenoid. The prosthetic is then coupled to the resected glenoid either with or without the attached central stem.

Use of the present invention provides an apparatus and method for shoulder arthroplasty, and specifically, a glenoid component and associated surgical components for use in shoulder arthroplasty. As a result, the aforementioned disadvantages associated with the currently available glenoid components and associated surgical components for shoulder arthroplasty have been substantially reduced or eliminated. It should be understood that the detailed description and specific examples, while indicating the preferred embodiment of the invention, are intended for purposes of illustration only and are not intended to limit the scope of the invention.

DRAWINGS

The drawings described herein are for illustration purposes only and are not intended to limit the scope of the present disclosure in any way.

FIG. 1 represents an exploded view of a modular glenoid according to the present teachings of the present disclosure;

FIG. 2 represents a second glenoid according to the present teachings;

FIGS. 3A and 3B represent perspective and side views of the glenoid according to FIG. 1;

FIGS. 4A and 4B represent perspective and side views of the glenoid according to FIG. 2;

FIGS. 5A and 5B represent alternate perspective and cross-sectional views according to the present teachings;

FIGS. 6A-6E represent perspective views of various stems usable in the glenoids shown in FIGS. 1-4B;

FIGS. 7A-7C represent various drive mechanisms;

FIGS. 8A-8E represent cross-sectional views of the stems shown in FIGS. 6A-6E;

FIGS. 9-12 represent perspective views of the preparation of the glenoid to accept the prosthetic shown in FIGS. 1-8E;

FIG. 13 represents the implantation of the glenoid shown in FIG. 1;

FIG. 14 represents a side cross-sectional view of a glenoid according to the present teachings implanted into a resected glenoid;

FIG. 15 represents a system of modular glenoid components according to the present teachings;

FIGS. 16 and 17 represent perspective and cross-sectional views of an alternate glenoid component according to the present teachings;

FIGS. 18A and 18B represent an integrally molded stem and glenoid component according to the present teachings;

FIGS. 19A and 18B represent perspective and cross-sectional views of a glenoid prosthetic according to the present teachings;

FIG. 20 represents a cross-sectional view of an alternate humeral head prosthetic according to the present teachings;

FIGS. 21-24 represent top and side views of various coupling members according to the present teachings; and

FIG. 25 represents a cross-sectional view of the coupling member shown in FIG. 22.

DETAILED DESCRIPTION

The following description is merely exemplary in nature and is not intended to limit the present disclosure, application, or uses.

Referring generally to FIGS. 1 and 2 which represent perspective views of the modular glenoid component according to the teachings of the present application. Shown is a glenoid prosthetic 20. The glenoid prosthetic 20 has a first side 22 having a generally spherical articulating surface 24 and a second coupling side 26. The spherical articulating surface 24 is adapted to permit rotational and translational movement of the head of the humeral component (not shown) or natural humerus. The coupling side 26 can include one or more fixed coupling stems 28 that are configured to couple the glenoid to a plurality of apertures defined within a resected glenoid.

The coupling stems 28 can be configured to include a first superior fixed peg 28 and a pair of second inferior fixed pegs 28, each fixed peg 28 positioned on the coupling side 26 to form the corners of a triangle and, preferably, an isosceles triangle. The coupling stems 28 can take on various forms. In this regard, the fixed stems 28 can have a relatively smooth profile which define annular and/or longitudinal grooves 33. As described below, the grooves 33 can be configured to accept bone cement to fixably couple the peg to apertures 35 defined within a resected glenoid 37. As shown in FIG. 2, the fixed glenoid stems 28 can have a plurality of aperture engaging flanges 31. Defined on the flanges 31 can be a plurality of grooves 39. These grooves 39 can be co-axial with grooves 33 defined by the stem 28.

As best seen in FIGS. 3A-3B, the coupling side 26 of the glenoid 20 also defines a central stem coupling mechanism 34. The coupling mechanism 34 is configured to removably and selectively couple a central fixation peg 48 to the coupling side 26. This mechanism can define male or female threaded portions which interface with the central stem 48. As shown, the coupling mechanism 34 can define a threaded coupling aperture 36 within a generally cylindrical body 38. As shown in FIGS. 4A-5B, this cylinder can have a flat or curved exterior surface. In this regard, it is envisioned the exterior surface can be tapered to transition into the coupling side 26. Disposed within the body 38 can be an internally threaded bushing 40. Defined on an exterior surface of the bushing 40 are optional coupling flanges 42 that are configured to couple the bushing 40 to the cylindrical body 38. This bushing can be coupled to the glenoid during a molding process, or the bushing can be press-fit into the coupling side 26.

FIGS. 6A-6E represent perspective and side views of the optional central coupling stems 48. Each of the central coupling stems 48 can have a threaded coupling member 50 which is configured to fixably interface the stem 48 with the threaded aperture 36 of the central coupling mechanism 34. The stems 48 further have a bearing surface or shoulder 51 configured to interface with a bearing surface or base 53 on the central coupling mechanism 34. Optionally, the stems 48 can have a textured coupling surface.

FIG. 6A represents a center peg 48 having a generally cylindrical fixation peg with an exterior powder metal coating. FIGS. 6B-6D represent central pegs having at least one aperture engaging flange. These flanges can either be used to interface with the interior of an aperture formed in the scapula or can be used to retain bone cement in the aperture. FIG. 6E represents a porous central peg having a stepped exterior surface. The stepped exterior surface has varying diameter portions.

As shown, the central stem 48 can have various surface treatments. It is envisioned the stem can be formed of a biocompatible polymer, metallic or ceramic. Additionally, the central pegs can have surface treatment such as powder metal spray coating or other porous structures to facilitate the ingrowth of bone. As shown in FIGS. 7A-7C, optionally, the stems 48 can have drive surfaces 57 defined on a surface of the stem 48. These drive surfaces 57 can be a multi-faceted extension or a multi-faceted surface defined within a bore in the stem 48.

Shown in FIGS. 8A-8E, the stem can have various cross-sections. In this regard, the diameters of the stems can vary along the length of the stems 48. As shown in FIGS. 6B-6D, the stems 48 can have various coupling flanges 55 incorporated thereon. These coupling flanges 55 can be configured to have an exterior diameter which is less than, equal to, or greater than the corresponding diameter of a portion of an aperture disposed in the resected glenoid 37. Each of the stems 48 is configured to interface with a bearing surface on the central coupling mechanism 34.

FIGS. 9-13 represent the preparation and insertion of the glenoid 20 according to the teachings herein. As shown in FIG. 9, a second drilling guide 64 can be used to position a central pilot hole 67 into the surface 62. After the preparation of a central guide hole 67, as shown in FIG. 10, the surface of the glenoid 62 is prepared using a rotating rasp or file 52. The scapula is then machined to form the resected glenoid 37. Shown is a rotating rasp 52 used to prepare a planar or curved glenoid surface to mate with the coupling side of the prosthetic 20.

After the resection, a plurality of fixed peg accepting holes 59 are machined into the resected glenoid 37. FIG. 11 represents the use of a drilling guide 56 for the placement of holes within the resected glenoid 37. In this regard, it is envisioned that the drilling guide 56 be used to position the apertures for the acceptance of the fixed stems 28. As shown in FIG. 12, immediately about a central pilot hole, a surface 66 is prepared which is configured to accept the stem coupling mechanism 34. The center stem accepting aperture can be formed either prior to or after the preparation of the surface 66 to accept the stem coupling mechanism 34. At this point, the physician can determine if a central fixation peg 48 is needed. If the central peg 48 is needed, the physician will further determine a preferred central peg fixation surface and a preferred central peg fixation size. The appropriate peg 48 is then chosen and theadably coupled to the glenoid 20 so as to cause engagement of the stem bearing surface 51 with the bearing surface 53 on the central coupling mechanism 34.

As shown in FIG. 13, it is envisioned that bone cement or biological materials can be injected into the apertures defined within the resected glenoid 37. These materials can be inserted into the holes configured to accept the fixed pegs or the central stem 48. It is equally envisioned that the central stem 48 can be inserted into the aperture so as to form an interference fit between the central stem 48 and the aperture. With the appropriate coupling stem 48 fixed to the bushing within the coupling mechanism 34, proper coupling of the glenoid 20 can occur. In this regard, the central stem 48 is threadably coupled to an aperture within the central stem coupling mechanism 34. The fixed and central stems are positioned within the apertures to couple the glenoid member 20 to the resected glenoid 37.

FIG. 14 represents a cross-sectional view of an implanted glenoid 20. Shown is the relationship between the articulating surface 24, fixed stems 28, and the central stem 48. Optionally, the coupling side 26 can be bonded to the resected glenoid using bone cement and further can have surface treatments to facilitate bonding. Further shown is the central stem 48 in relation to the threaded aperture 36 of the central stem coupling mechanism 34.

FIG. 15 represents a system of prosthetic components as described above. Shown are various glenoid prosthetics 20 as well as various size and shaped central stem portions 48. These stems 48 have various exterior surface treatments and configurations as well as varying lengths and diameters. It is envisioned that the system also includes the appropriate types of bone fixation cement, cutting members, cutting pattern guides, as well as humeral head and fixation stem prosthetics.

Referring generally to FIGS. 16 and 17 which represent perspective and cross sectional views of the modular glenoid component according to an alternate teaching. Shown is a glenoid prosthetic 20. The glenoid prosthetic 20 has a first side 22 having a generally spherical articulating surface 24 and a second coupling side 26. The spherical articulating surface 24 is adapted to permit rotational and translational movement of the head of the humeral component (not shown) or natural humerus. The coupling side 26 can include one or more removable peripheral coupling stems 28 that are configured to couple the glenoid to a plurality of apertures defined within a resected glenoid.

The coupling stems 28 can be configured to include a first superior removable peg 28 and a pair of second inferior removable pegs 28. Each removable peg 28 is positioned on the coupling side 26 to form the corners of a triangle and, optionally, an isosceles triangle. The coupling pegs 28 can take on various forms. In this regard, the pegs 28 can have a relatively smooth profile which define annular and/or longitudinal grooves 33. As described above, the grooves 33 can be configured to accept bone cement to fixably couple the peg to apertures 35 defined within a resected glenoid 37. As shown in FIG. 17, the fixed glenoid stems 28 can have a porous outer coating such as Regenerex (see also FIG. 8A).

It is envisioned that the pegs 28 can be coupled to the coupling side via a threaded member or a locking taper. The threaded member 60 can have a self tapping thread configured to engage a threaded hole formed in the coupling side 26. Additionally, the threaded member 60 can be coupled to a bushing integrally molded into the glenoid prosthetic 20. Optionally, the threaded bushing can have a textured exterior surface or retaining flange to facilitate the integration thereof. Each peg has a flat bearing surface configured to bear against a flat bearing surface on the medial side or the bushing.

As shown in FIGS. 18A and 18B, the coupling stem 48 can be integrally molded into the glenoid prosthetic 20. In this regard, the premachined stem 48 can have a porous coating integrally formed thereon. Additionally formed on the stem 28 can be a plurality of flanges used to fix the coupling stem into the glenoid prosthetic and protruding from the coupling surface 26. As described above, the central fixation stem can be coupled to the threaded central bore 36 formed in the plastic or an inserted bushing.

As shown in FIG. 18B, the stem 28 can be formed of a titanium substrate 70 with an applied Regenerex layer. The Regenerex layer can be machined prior to being placed within a mold. A blank which is used to form the glenoid body 20 can then be formed by molding an e-poly block over the titanium stem substrates. The polymer can be formed of sintered UHMWPE 1050 powder. This polymer can be doped with vitamin E for six hours and then homogenized for 400 hours. The polymer can then be machined into final form after molding. In this regard, the bearing and interface surfaces 24, 20 can be machined into the glenoid prosthetic 20.

FIGS. 19A and 19B represent perspective and cross sectional views of the modular glenoid component according to an alternate teaching. The glenoid prosthetic 20 has a first side 22 having a generally spherical articulating surface 24 and a second coupling side 26. The spherical articulating surface 24 is adapted to permit rotational and translational movement of the head of the humeral component (not shown) or natural humerus. The coupling side 26 can be formed of a tray 62 which includes one or more fixed peripheral coupling stems 28 that are configured to couple the glenoid to a plurality of apertures defined within a prepared glenoid. The polymer bearing can be integrally molded onto the tray 62, or can be snapped onto the tray 62 using a snap feature 64. Alternatively, the bearing can be coupled to the tray 62 using integral coupling pegs 68. The tray incorporated pegs 68 can have surface treatments or flanges to facilitate fixation.

FIG. 20 represents a cross-sectional view of an alternate humeral component according to the present teachings. Shown is a resected humerus 74 having a coupling member 76 disposed therein. The coupling member 76 has a generally cylindrical body 78 having a plurality of bone engaging flanges 80 disposed thereon. The generally cylindrical body 78 has an outer surface having a generally constant exterior diameter. Disposed at a proximal end 82 of the body is a generally planar and circular head coupling surface 86. The head coupling surface 86 has an associated coupling taper 88 configured to couple a humeral head 92 to the coupling member 76.

As shown in FIGS. 21 and 23, the body can have a circular or an oblong circular cross-sectional shape. It is envisioned the shape can be formed into the resected humerus 74 using a rotating cutting member and a cutting measurement guide. The coupling member 76 can be impacted into an aperture formed into the resected head or head and neck of the humerus 74. In this regard, an impaction tool (not shown) can be coupled to a threaded hole 88 defined within the body. Slots can be formed into the humerus 74 to accept the retaining flanges therein. Optionally, the entire prosthetic can be placed within only the head or head and neck, and not into the medullary canal.

As shown in FIGS. 24 and 25, the exterior surface of the body can be uncoated or at least be partially coated with metallic powder coating, or coatings such as Regenerex, configured to promote boney in-growth. This powder metal or bone growth promoter can also cover the generally planar interface surface 90 at the distal end 92 of the coupling member.

Example embodiments are provided so that this disclosure will be thorough, and will fully convey the scope to those who are skilled in the art. Numerous specific details are set forth such as examples of specific components, devices, and methods, to provide a thorough understanding of embodiments of the present disclosure. It will be apparent to those skilled in the art that specific details need not be employed, that example embodiments may be embodied in many different forms and that neither should be construed to limit the scope of the disclosure. In some example embodiments, well-known processes, well-known device structures, and well-known technologies are not described in detail.

The terminology used herein is for the purpose of describing particular example embodiments only and is not intended to be limiting. As used herein, the singular forms “a”, “an” and “the” may be intended to include the plural forms as well, unless the context clearly indicates otherwise. The terms “comprises,” “comprising,” “including,” and “having,” are inclusive and therefore specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. The method steps, processes, and operations described herein are not to be construed as necessarily requiring their performance in the particular order discussed or illustrated, unless specifically identified as an order of performance. It is also to be understood that additional or alternative steps may be employed.

When an element or layer is referred to as being “on”, “engaged to”, “connected to” or “coupled to” another element or layer, it may be directly on, engaged, connected or coupled to the other element or layer, or intervening elements or layers may be present. In contrast, when an element is referred to as being “directly on,” “directly engaged to”, “directly connected to” or “directly coupled to” another element or layer, there may be no intervening elements or layers present. Other words used to describe the relationship between elements should be interpreted in a like fashion (e.g., “between” versus “directly between,” “adjacent” versus “directly adjacent,” etc.). As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.

Although the terms first, second, third, etc. may be used herein to describe various elements, components, regions, layers and/or sections, these elements, components, regions, layers and/or sections should not be limited by these terms. These terms may be only used to distinguish one element, component, region, layer or section from another region, layer or section. Terms such as “first,” “second,” and other numerical terms when used herein do not imply a sequence or order unless clearly indicated by the context. Thus, a first element, component, region, layer or section discussed below could be termed a second element, component, region, layer or section without departing from the teachings of the example embodiments.

Spatially relative terms, such as “inner,” “outer,” “beneath”, “below”, “lower”, “above”, “upper” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. Spatially relative terms may be intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is turned over, elements described as “below” or “beneath” other elements or features would then be oriented “above” the other elements or features. Thus, the example term “below” can encompass both an orientation of above and below. The device may be otherwise oriented (rotated 90 degrees or at other orientations)

Claims

1. A system for use during shoulder arthroplasty, said system having a glenoid component adapted to be implanted into a scapula and engaged by a head of a humeral component, said glenoid component comprising:

a body having a first articulating surface and a second medial surface opposite said first articulating surface, said first articulating surface adapted to be engaged by a humeral head and said second medial surface adapted to be secured to the scapula, a generally cylindrical coupling mechanism protruding from said second medial surface, said coupling mechanism having first and second flat bearing surfaces;

a first metal bushing integrally molded within the coupling mechanism, said metal bushing defining a first threaded central bore;

a second metal bushing integrally molded within the coupling mechanism, said second metal bushing defining a second threaded bore;

at least one removable peg, having a first end adapted to non-rotatably engage a cavity formed in the scapula and a second end fixably coupled to said first metal bushing and extending from said medial surface; and

a removable stem having a third exterior flat bearing surface configured to interface with the second flat bearing surface when the removable stem is engaged with the second threaded bore before the body is engaged with the scapula, said removable stem being configured to be non-rotatably engaged with a hole defined in the scapula.

2. The system as defined in claim 1 wherein said first articulating surface has a spherical concave surface adapted to permit rotational and translational movement of the head of the humeral component.

3. The system as defined in claim 1 wherein said second removable stem includes a textured coupling surface.

4. The system as defined in claim 3 wherein said textured coupling surface includes one of a porous coating or a porous metal.

5. The system as defined in claim 1 wherein the at least one removable peg defines at least one of a bone cement retaining groove and a plurality of bone cement retaining flanges.

6. The system as defined in claim 1 wherein said at least one removable peg includes a first superior removable peg and a pair of second inferior removable pegs, each removable peg positioned on said second medial surface to form the corners of an isosceles triangle.

7. The system as defined in claim 1 wherein a central stem is defined by a generally cylindrical outer peripheral surface, said central stem including a fixation thread.

8. The system as defined in claim 1 wherein each of said at least one removable pegs includes a textured surface.

9. The system as defined in claim 1 comprising a plurality of central fixation pegs.

10. A system for use in shoulder arthroplasty, said system having a glenoid component adapted to be implanted into a scapula, said system comprising:

a body having a first articulating surface and a second medial surface opposite said first articulating surface, said second medial surface adapted to be secured to the scapula;

a peripheral cylindrical stem coupling mechanism having a fixed metal bushing integrally molded within the peripheral cylindrical stem coupling mechanism defining a threaded aperture disposed therein, said peripheral cylindrical stem coupling mechanism defining a coupling aperture in the second medial surface; and

a plurality of peripheral stems removably and selectively couplable to the peripheral cylindrical stem coupling mechanism, wherein the peripheral stems vary in size, one of said plurality of stems a flat exterior bearing surface configured to engage the peripheral cylindrical stem coupling mechanism.

11. The system as defined in claim 10 wherein one of said peripheral stems includes an enhanced textured surface.

12. The system as defined in claim 11 wherein said enhanced textured surface includes a porous coating.

13. The system as defined in claim 10 wherein the second medial surface comprises a removable central stem which defines a bone cement retaining groove.

14. The system as defined in claim 13 wherein the removable stem defines a plurality of bone cement retaining flanges.

15. The system as defined in claim 13 wherein said plurality of peripheral pegs comprise a first superior removable peg and a pair of second inferior removable pegs.

16. The system as defined in claim 10 wherein the peripheral stem coupling mechanism is defined by a generally cylindrical outer peripheral surface.

17. The system as defined in claim 10 wherein the metal bushing has a retaining ring.

18. The system according to claim 10 further comprising a humeral prosthetic, said humeral prosthetic having a generally cylindrical coupling member configured to be positioned only within a resected humeral head or humeral head and neck, said coupling body having a generally constant exterior radius and a generally planar circular head coupling surface.

19. A method for implanting a medical device, the method comprising:

shaping a scapula to receive a glenoid prosthetic;

selecting a plurality of peripheral fixation pegs from a plurality of pegs;

coupling the plurality of peripheral fixation pegs to a plurality of bores defined by a plurality of fixed metal bushings integrally molded within a generally cylindrical coupling mechanism of a glenoid prosthetic so as to position a coupling mechanism bearing surface on the peripheral fixation peg against a peripheral fixation peg bearing surface on one of the metal bushings; and

coupling the glenoid prosthetic to the scapula after coupling the plurality of peripheral fixation pegs to the glenoid prosthetic,

wherein coupling the plurality of peripheral fixation pegs further includes determining at least one of an appropriate peripheral peg fixation surface and a peripheral peg fixation size.

20. The method according to claim 19 wherein coupling the plurality of peripheral fixation pegs is threadably coupling the plurality of peripheral fixation pegs to a plurality of threaded apertures defined by the plurality of metal bushings.

21. The method according to claim 19 further comprising shaping a plurality of peripheral fixation peg accepting apertures within the scapula.

22. The method according to claim 21 further comprising placing bone cement within the plurality of peripheral fixation peg accepting apertures.

23. The method according to claim 19 further comprising selecting a central fixation peg having an appropriate central fixation peg fixation surface.